A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6577391



Internal ID20950462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:25781211..25781574hg38UCSC Ensembl
chr13:26355349..26355712hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg38364
hg19364
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220514
Samples
Known GenesATP8A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6577391
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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